Moyamoya disease is a rare, progressive cerebrovascular disorder characterized by the narrowing of the internal carotid arteries and their branches, leading to the development of tiny, fragile blood vessels which can easily rupture. Type 5 Moyamoya disease, associated with mutations in the ACTA2 gene, is a particular form of this condition that not only affects […]
ACTA2 gene multisystemic smooth muscle dysfunction syndrome is a rare genetic disorder that affects the smooth muscles throughout the body. This condition is caused by mutations in the ACTA2 gene, which plays a crucial role in the contraction and function of smooth muscle cells. These mutations lead to a wide range of symptoms and complications, […]
Myopathy refers to a group of diseases that affect the muscle fibers, leading to weakness, cramps, stiffness, and even spasms. One specific form of myopathy is linked to mutations in the mitochondrial transfer RNA (tRNA) genes, including the MT-TQ gene. This article delves into the symptoms associated with MT-TQ gene myopathy and the importance of […]
At DNA Labs UAE, we specialize in providing comprehensive genetic testing services that cater to a wide range of genetic disorders. One such critical test we offer is for the MIB1 gene associated with Left Ventricular Noncompaction 7 (LVNC7). This condition is a rare form of cardiomyopathy that affects the structure of the heart, leading […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and management. Among these, the FBN1 gene mutation leading to MASS syndrome represents a significant concern due to its varied symptoms and impact on multiple body systems. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive solutions including the FBN1 Gene […]
Understanding the TLR5 Gene and Its Role in Legionnaire Disease Susceptibility Legionnaire’s disease, a severe form of pneumonia caused by the Legionella bacteria, can be life-threatening if not diagnosed and treated promptly. While the bacteria can infect anyone, certain individuals are more susceptible due to genetic factors. Recent advancements in genetic testing have shed light […]
Understanding KCNQ1 Gene Long QT Syndrome Type 1 Long QT Syndrome (LQTS) is a disorder of the heart’s electrical activity that can cause sudden, uncontrollable, and dangerous arrhythmias. These arrhythmias may lead to fainting, seizures, or even sudden death. Among the several genetic variants of LQTS, the Type 1, associated with mutations in the KCNQ1 […]
Understanding the symptoms and genetic underpinnings of Long QT Syndrome Type 10 (LQTS10) is crucial for individuals and families affected by this condition. The SCN4B gene plays a significant role in this type of Long QT Syndrome, a disorder that can lead to severe cardiac events. At DNA Labs UAE, we offer a comprehensive genetic […]
Long QT Syndrome (LQTS) is a heart rhythm disorder that can potentially lead to fast, chaotic heartbeats. These rapid heartbeats might trigger a sudden fainting spell or seizure. In some cases, the heart’s rhythm may be so erratic that it can cause sudden death. Among the various genetic forms of this condition, Long QT Syndrome […]
Symptoms of SNTA1 Gene Long QT Syndrome Type 12 Long QT Syndrome Type 12, associated with mutations in the SNTA1 gene, is a rare inherited condition that can lead to serious heart rhythm abnormalities. It is crucial for individuals to be aware of the symptoms associated with this condition to seek timely medical intervention. The […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
